참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diphenylamine | HCID 11487 | — |
| 반응물 | Di-tert-butylchlorophosphine | HCID 139566 | — |
| 반응물 | Benz(a)anthracene, 4-bromo- | HCID 182324 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(Diphenylamino)benz[a]anthracene | HCID 59412792 | — |
반응 단계
190 μl (1 mmol) of chlorodi-tert-butylphosphine and then 112 mg (0.5 mmol) of palladium(II) acetate are added to a suspension of 15.4 g (50 mmol) of 4-bromobenz[a]anthracene, 10.2 g (60 mmol) of diphenylamine and 7.7 g (80 mmol) of sodium tert-butoxide in 500 ml of toluene, and the mixture is subsequently heated under reflux for 5 h. After the mixture has been cooled to 60° C., 500 ml of water are added, the organic phase is separated off, filtered through silica gel, evaporated virtually to dryness at 80° C. in vacuo, and 300 ml of ethanol are then added. After cooling, the solid is filtered off with suction. Recrystallisation five times from dioxane (about 8 ml/g); sublimation (p=5×10−5 mbar, T=280° C.). Yield: 12.7 g (32 mmol), 64.1%, purity 99.9% (HPLC), Tg=74.7° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08986852B2 |
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| 출처 데이터셋 | uspto-grants-2015_03 |
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| ORD ID | ord-3d424e238af145848f7273db027f9b8e |
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| 출처 메모 | uspto-grants-2015_03 |
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